Infantile neuroaxonal dystrophy and its relationship to Hallervorden‐Spatz disease

Abstract
A case of in-fantile neuroaxonal dystrophy is compared with 3 cases of infantile Hallervorden-Spatz disease, clinically and pathologically. Attention is drawn to relatively frequent association between the 2 disorders but it is suggested that tentatively the 2 conditions can be regarded as separate entities.

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